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Biomedical subjects

J Simpson

Publications and source records attributed to J Simpson.

At least 325 records · Page 18Linked to original sources
PubMed1979

A case of maturity-onset diabetes mellitus resistant to insulin but responsive to tolbutamide.

A nonobese patient with maturity-onset diabetes mellitus was hospitalized for treatment of an ulcer on his right foot. During this episode, his diabetic control worsened, and he proved unresponsive to exogenous insulin. Unresponsiveness to insulin persisted after healing of the ulcer. Tolbutamide therapy was then begun and produced a marked reduction in blood sugar levels. Withdrawal of the drug was accompanied by a progressive rise in blood sugar level. Intravenous infusion of regular pork insulin at rates of 45 U/h and single-component pork insulin at rates of 120 U/h had minimal effect on the blood sugar level. High levels of antibody to beef insulin were measured, with lower levels of pork insulin antibodies. C-peptide values were in a normal range before tolbutamide treatment and increased after use of the drug.

Administration, Oral↗
PubMed1977

Partial trisomy 14q -- and parental translocation of No. 14 chromosome. Report of a case and review of the literature.

A case of partial trisomy 14 (47, + 14q-) is presented. The proband's mother had a balanced translocation of 14q with the long arm of a No. 3 chromosome. Clinical and cytogenetic findings of this case are compared with 5 other cases of 47, + 14q-, in which one parent had a balanced translocation of the distal part of the No. 14 long arm to another chromosome. It appears that this chromosomal aneuploidy produces a fairly typical clinical picture.

Chromosome Aberrations↗
PubMed1977

Oral health of airmen: analysis of panoramic radiographic and Polaroid photographic survey.

An oral health survey of 5,783 basic airmen was conducted. In this study, emphasis was placed on detection of periodontal disease. Numerous pathologic conditions were found and recorded. In addition, the presence or absence of evidence of previous dental care and its nature were reported. We believe that panoramic radiographs and Polaroid intraoral photographs have merit in mass screening of large numbers of persons for the detection of periodontal disease. Through the use of these diagnostic aids, various degrees of periodontal disease could be diagnosed. Other pathologic entities that might have been missed with routine dental radiographs were observed. However, although the diagnostic aids used in this report are a helpful adjunct, in their present state of development they should not be used to replace standard dental radiographs and clinical examination.

Aerospace Medicine↗
PubMed1976

The problem of trisomy 22. A case report and a discussion of the variant forms.

A case of trisomy 22 with partial long arm deletion (47, +22 q-) studied by G-banding is presented. The patient, a five-month-old male, showed failure to thrive, delayed psychomotor development, large, low-set ears, mild micrognathia, atrial septal defect, and marked muscular hypotonia. The father's karyotype was normal. The mother's karyotype was 46 XX, but one of the no22 chromosomes showed a deletion of the long arm as seen in the proband's karyotype. A comparison with previously reported cases in the literature indicates a great variability of clinical features of trisomy 22: "classical form," cat eye syndrome, and abortive cases (as this reported case).

Abnormalities, Multiple↗
PubMed1975

Trisomy 22.

The existence of a trisomy 22 has been definitely established by newer methods of karyotype analysis which permit distinction between the acrocentric chromosomes of group G. Trisomy 22 is much rarer than trisomy 21. This report presents presumptive evidence that the cat eye syndrome (CES), the so-called "trisomy 22" (T22), the intermediate cases (IM) with cardinal symptoms of CES and T22, and some cases of mental retardation with rather unspecific symptoms are variants of the same disease entity. For T22, CES and one abortive case the extra chromosome was clearly identified as number 22 chromosome with or without partial deletion of the long arm. An interesting and presently not fully understood feature of trisomy 22 is its frequent familial incidence.

Abnormalities, Multiple↗